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Effect of pH on microbial degradation of leaf litter in seven streams of the English Lake District

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Summary

Rates of degradation of alder, oak and grass leaf packs with associated microbial populations were measured in seven streams pH 6.8–4.9. Streams were chosen from upland and lowland sites of the same river for contrasts in pH, water chemistry and riparian vegetation. The most important factor governing rates of degradation is the physical and chemical nature of the leaf material. At pH 6.8 rates of degradation, ‘k’, and microbial colonization were higher than at pH \(\bar <\)5.5: ‘k’ on alder x6; on oak x2; on grass x2. At lowland sites, pH 6.8, higher decay rates were associated with high levels of microbial colonization including c.14 spp of aquatic hyphomycete fungi—regardless of riparian vegetation. Decay rates were similar at upland sites, pH 6.8 and 6.6, involving high levels of colonization by fewer fungal species and fewer bacteria—regardless of riparian vegetation-though grass was barely degraded at upland sites of any pH. At pH\(\bar <\)5.5, slow decay rates were associated with low levels of microbial colonization and few fungal species. Largest microbial populations at low pH associated with riparian trees did not lead to markedly increased decay rates. Factors of water chemistry at low pH appear to inhibit microbial metabolism. The implications of these findings for stream invertebrates active in the winter is discussed.

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References

  • Anderson NH, Sedell JR (1979) Detritus processing by macroinvertebrates in stream ecosystems. Ann Rev Entomol 24:351–377

    Google Scholar 

  • Barlocher F, Kendrick B (1974) Dynamics of the fungal population on leaves in a stream. J Ecol 62:761–791

    Google Scholar 

  • Baker JH, Bradnam LA (1976) The role of bacteria in the nutrition of aquatic detritivores. Oecologia (Berlin) 24:95–104

    Google Scholar 

  • Carrick TR, Sutcliffe DW (1983) Concentrations of major ions in streams on catchments of the River Duddon (1971–1974) and Windermere (1975–1978), English Lake District. Freshwater Biological Association Occasional Publication No. 21

  • Chamier A-C (1985) Cell-wall degrading enzymes of aquatic hyphomycetes: a review. Bot J Linn Soc 91:67–81

    Google Scholar 

  • Chamier A-C, Dixon PA (1982a) Pectinases in leaf degradation by aquatic hyphomycetes I. The field study: the colonization-pattern of aquatic hyphomycetes on leaf packs in a Surrey stream. Oecologia (Berlin) 52:109–115

    Google Scholar 

  • Chamier A-C, Dixon PA (1982b) Pectinases in leaf degradation by aquatic hyphomycetes: the enzymes and leaf maceration. J Gen Microbiol 128:2469–2483

    Google Scholar 

  • Chamier A-C, Willoughby LG (1986) The role of fungi in the diet of the amphipod Gammarus pulex (L.): an enzymatic study. Freshwat Biol 16:197–208

    Google Scholar 

  • Chamier A-C, Dixon PA, Archer SA (1984) The spatial distribution of fungi on decomposing alder leaves in a freshwater stream. Oecologia (Berlin) 64:92–103

    Google Scholar 

  • Cummins KW, Klug MJ (1979) Feeding ecology of stream invertebrates. Ann Rev Ecol Syst 10:147–172

    Google Scholar 

  • Cummins KW, Petersen RC, Howard FO, Wuycheck JC, Holt VI (1973) The utilisation of leaf litter by stream detritivores. Ecology 54:336–345

    Google Scholar 

  • Darnell RM (1964) Organic detritus in relation to secondary production in aquatic communities. Verh int ver theor angew Limnol 15:462–470

    Google Scholar 

  • Egglishaw HJ (1964) The distributional relationship between the bottom fauna and plant detritus in streams. J Animal Ecol 33:463–476

    Google Scholar 

  • Elliott JM, Minshall GW (1968) The invertebrate drift in the River Duddon, English Lake District. Oikos 19:39–52

    Google Scholar 

  • Evans JH (1972) A modified sedimentation system for counting algae with an inverted microscope. Hydro Biol 40:207–250

    Google Scholar 

  • Fisher SG, Likens GE (1973) Energy flow in Bear Brook, New Hampshire: an integrated approach to stream ecosystem metabolism. Ecol Monogr 43:421–439

    Google Scholar 

  • Friberg F, Otto C, Svensson B (1980) Effects of acidification on the dynamics of allochthonous leaf material and benthic invertebrate communities in running water. In: Drablos D, Tollan A (eds), Ecological Impact of Acid Precipitation. Proc int Conf Oslo Norway SNSF Project 304-305

  • Hall CAS (1972) Migration and metabolism in a temperate stream ecosystem. Ecology 53:585–604

    Google Scholar 

  • Howarth RW, Fisher SG (1976) Carbon, nitrogen and phosphorous dynamics during leaf decay in nutrient enriched stream micro-ecosystems. Freshwat Biol 6:221–228

    Google Scholar 

  • Hynes HBN (1961) The invertebrate fauna of a Welsh mountain stream. Arch Hydrobiol 57:344–388

    Google Scholar 

  • Hynes HBN, Kaushik NK, Lock MA, Lush DR, Stockner Z StJ, Wallace RR, Williams DD (1974) Benthos and allochthonous organic matter in streams. J Fish Res Board Canada 31:545–553

    Google Scholar 

  • Ingold CT (1979) Advances in the study of so-called aquatic hyphomycetes. Amer J Bot 66:218–226

    Google Scholar 

  • Iqbal SH, Webster J (1973) Aquatic hyphomycete spora of the River Exe and its tributaries. Trans Br mycol Soc 61:331–346

    Google Scholar 

  • Iqbal SH, Webster J (1977) Aquatic hyphomycete spora of some Dartmoor streams. Trans Br mycol Soc 69:233–241

    Google Scholar 

  • Jones JG, Simon BM (1975) An investigation of errors in direct counts of aquatic bacteria by epifluorescence microscopy, with reference to a new method of dyeing membrane filters. J appl Bact 39:317–329

    Google Scholar 

  • Kaushik NK, Hynes HBN (1971) The fate of dead leaves that fall into streams. Arch Hydrobiol 68:1465–1515

    Google Scholar 

  • Mackay RJ, Kersey KE (1985) A preliminary study of aquatic insect communities and leaf decomposition in acid streams near Dorset, Ontario. Hydrobiologia 122:3–11

    Google Scholar 

  • Malmquist B, Nilsson LM, Svensson BS (1978) Dynamics of detritus in a small stream in Southern Sweden and its influence on the distribution of the bottom animal communities. Oikos 31:3–16

    Google Scholar 

  • Meyer JL (1980) Dynamics of phosphorous and organic matter during leaf decomposition in a freshwater stream. Oikos 34:44–53

    Google Scholar 

  • Minshall GW (1967) Role of allochthonous detritus in the trophic structure of a woodland springbrook community. Ecology 48:139–149

    Google Scholar 

  • Minshall GW, Keuhne RA (1969) An ecological study of invertebrates of the Duddon, an English mountain stream. Arch Hydrobiol 66:169–191

    Google Scholar 

  • Minshall GW, Minshall JN (1978) Further evidence of the role of chemical factors in determining the distribution of benthic invertebrates in the River Duddon. Arch Hydrobiol 83:324–355

    Google Scholar 

  • Petersen RC, Cummins KW (1974) Leaf processing in a woodland stream. Freshwat Biol 4:343–368

    Google Scholar 

  • Shearer CA, Webster J (1985a, b, c) Aquatic hyphomycete communities in the River Teign. I. Longitudinal distribution patterns. Trans Br mycol Soc 84:489–501 II. Comparison of sampling techniques. Trans Br mycol Soc 84:503–507 III. Temporal distribution patterns. Trans Br mycol Soc 84:509–518

    Google Scholar 

  • Sutcliffe DW (1983) Acid precipitation and its effects on aquatic systems in the English Lake District (Cumbria). Rep Freshwat biol Ass No. 51, 30–62

  • Sutcliffe DW, Carrick TR (1973) Studies on mountain streams in the English Lake District I. pH, calcium and the distribution of invertebrates in the River Duddon. Freshwat Biol 3:437–462

    Google Scholar 

  • Sutcliffe DW, Carrick TR, Willoughby LG (1981) Effects of diet, body size, age and temperature on growth rates in the amphipod Gammerus pulex. Freshwat Biol 11:183–214

    Google Scholar 

  • Townsend CR, Hildrew AG, Francis J (1983) Community structure in some southern English streams and the influence of physicochemical factors. Freshwat Biol 13:521–544

    Google Scholar 

  • Traaen TS (1980) Effects of acidity on decomposition of organic matter in aquatic environments. In: Drablos D, Tollan A (eds), Ecological Impact of Acid Precipitation. Proc int Conf Oslo Norway. SNSF Projet 340-341

  • Triska FJ, Sedell JR, Buckley B (1975) The processing of conifer and hardwood leaves in two coniferous forest streams II. Biochemical and nutrient changes. Verh Int Verein Limnol 19:1628–1639

    Google Scholar 

  • Willoughby LG, Sutcliffe DW (1976) Experiments on feeding and growth of the amphipod Gammarus pulex (L.) related to its distribution in the River Duddon. Freshwat Biol 6:577–586

    Google Scholar 

  • Zimmermann R, Iturriaga R, Becker-Birck J (1978) Simultaneous determination of the total number of aquatic bacteria and the number there of involved in respiration. Appl environ Microbiol 36:926–935

    Google Scholar 

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Chamier, A.C. Effect of pH on microbial degradation of leaf litter in seven streams of the English Lake District. Oecologia 71, 491–500 (1987). https://doi.org/10.1007/BF00379287

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